Canonical Allele Identifier: CA392977941

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335836-A-G
• MyVariant Identifiers: chr15:g.68628174A>G (hg19) ; chr15:g.68335836A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335836A>G , CM000677.2:g.68335836A>G	GRCh38
NC_000015.9:g.68628174A>G , CM000677.1:g.68628174A>G	GRCh37
NC_000015.8:g.66415228A>G	NCBI36
NG_046911.1:g.101325T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000315757.9:c.1286T>C MANE Select	ENSP00000327290.7:p.Val429Ala
ENST00000315757.8:c.1286T>C	ENSP00000327290.7:p.Val429Ala
ENST00000423218.6:c.1286T>C	ENSP00000403392.2:p.Val429Ala
ENST00000566429.1:n.197-22T>C
ENST00000569346.5:n.265T>C
NM_001004439.1:c.1286T>C	NP_001004439.1:p.Val429Ala
XM_005254228.2:c.980T>C	XP_005254285.1:p.Val327Ala
XM_011521363.1:c.1079T>C	XP_011519665.1:p.Val360Ala
XM_005254228.3:c.980T>C	XP_005254285.1:p.Val327Ala
XM_011521363.2:c.1079T>C	XP_011519665.1:p.Val360Ala
NM_001004439.2:c.1286T>C MANE Select	NP_001004439.1:p.Val429Ala